HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698952Erstellt: 25. Oktober 2026
Hexane → 6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazoline
https://huagongshe.com/reaction/1698952
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 4-(Dimethylamino)butan-1-ol | HCID 83350 | — |
| Edukt | N-(3-Bromophenyl)-7-fluoro-6-nitroquinazolin-4-amine | HCID 10761182 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Methylenechloride Hexane | HCID 21226440 | — |
| Lösungsmittel | Ethylacetate methanol | HCID 21584119 | — |
| Produkt | 6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazoline | HCID 10693912 | 33% |
Reaktionsschritte
To a suspension of hexane prewashed sodium hydride (11.0 mmol, 440 mg of a 60% dispersion in mineral oil) in THF (20 mL) was cannulated a solution of 4-(N,N-dimethylamino)butan-1-ol (8.80 mmol, 1.03 g) in THF (30 mL). The resulting suspension was stirred at 20° C. under N2 for 2 hours and then cannulated into a solution of 4-[(3-bromophenyl)amino]-7-fluoro-6-nitroquinazoline (J Med Chem, 1996;39:918-928) (0.80 g, 2.20 mmol) in THF (30 mL) under N2. The dark red solution was then heated at reflux overnight. Identical workup as above gave, after chromatography on grade III alumina eluting with EtOAc to MeOH/EtOAc (5:95) to give 6-amino-4-[(3-bromophenyl)amino]-7-[4(N,N-dimethylamino)butyloxy]quinazoline (310 mg, 33%) as a pale brown powder, mp (CH2Cl2/hexane) 155-156° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06344459B1 |
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| Quelldatensatz | uspto-grants-2002_02 |
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| ORD ID | ord-338a8fee1d5d47ad95776c56a158f484 |
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| Quellennotiz | uspto-grants-2002_02 |
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